FDA inspection

KYOCERA Corporation Shiga Higashiomi Plant Block 2: FDA inspection ending Feb 27, 2014

FDA inspection 872247 · No Action Indicated (NAI) · Higashiomi

Key facts

Inspection ID 872247
Firm KYOCERA Corporation Shiga Higashiomi Plant Block 2
FEI number 3006536454
Address Kyosera (Kabu) Shigakojo, Shigakojo; Kawai-Cho
City Higashiomi
Country Japan
Fiscal year 2014
Inspection end date Feb 27, 2014
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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